[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100530020":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":25,"centralContacts":29,"locations":35,"responsibleParty":62,"collaborators":64,"id":68,"slug":69,"hasResults":70,"nctId":71,"briefTitle":72,"officialTitle":73,"acronym":18,"eligibilityCriteria":74,"healthyVolunteers":70,"sex":75,"minAge":76,"maxAge":18,"enrollmentInfo":77,"targetDuration":18,"studyType":80,"phases":81,"briefSummary":83,"conditions":84,"keywords":87,"overallStatus":38,"whyStopped":18,"lastUpdateSubmitDate":90,"lastUpdatePostDateStruct":91,"startDateStruct":94,"completionDateStruct":96,"leadSponsor":98,"locationsCount":99},{"fullName":5,"class":6},"The University of Hong Kong","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"implementation condition","EXPERIMENTAL","Under implementation condition, a fear of cancer recurrence screening program will be implemented in routine oncological clinics using 5 implementation strategies including training, audit and feedback, facilitation and adaptable workflow.",[13],"Behavioral: FCR screening and referral program",{"label":15,"type":16,"description":17,"interventionNames":18},"Control condition","NO_INTERVENTION","In the control condition, the clinical outpatient operation is performed as usual. The FCR screening tool and referral forms will be provided to the study sites and nursing staff are encouraged to adopt fear of cancer recurrence screening. Patients referred to JCICC will be managed following the predefined clinical pathway triage system. A briefing session about the purpose of the implementation program and the introduction of the FCR screening tool will be given to the staff at each study unit before the start of the first 4-months control condition. The briefing session will be recorded for the purpose of fidelity assessment.",null,[20],{"type":21,"name":22,"description":23,"armGroupLabels":24,"otherNames":18},"BEHAVIORAL","FCR screening and referral program","Five implementation strategies will be conducted individually for each of the study unit at the timepoint when the study unit is being randomly allocated to the implementation condition. For each study unit, all nurses will first receive a half-day training. Each study unit under the implementation condition will receive weekly audit and feedback reports to summarize the proportion of eligible patients, proportion of eligible patients being screened, proportion of patients appropriately referred to JCICC. The senior research assistant with a nursing background will receive training and mentoring from the PI and will be the guided facilitator. The guided facilitator will conduct weekly site visits to address operational issues arise during the implementation. Lastly, while the choice of symptom assessment tool and referral criteria are standardized and cannot be modified, the routine workflow for each study unit can be adjusted according to its context and resources.",[9],[26],{"name":27,"affiliation":5,"role":28},"Danielle Ng, PhD","PRINCIPAL_INVESTIGATOR",[30],{"name":31,"role":32,"phone":33,"phoneExt":18,"email":34},"Danielle Ng, Phd","CONTACT","+852 39179897","dwlng@hku.hk",[36,52],{"facility":37,"status":38,"city":39,"state":18,"zip":18,"country":39,"countryCode":40,"cosmosGeoPoint":41,"geoPoint":46,"contacts":47},"KWH Breast clinic","RECRUITING","Hong Kong","HK",{"type":42,"coordinates":43},"Point",[44,45],114.17469,22.27832,{"lat":45,"lon":44},[48],{"name":49,"role":32,"phone":50,"phoneExt":18,"email":51},"Vanessa Chun","85246585123","cok702@ha.org.hk",{"facility":53,"status":38,"city":39,"state":18,"zip":18,"country":39,"countryCode":40,"cosmosGeoPoint":54,"geoPoint":56,"contacts":57},"QMH department of Surgery",{"type":42,"coordinates":55},[44,45],{"lat":45,"lon":44},[58],{"name":59,"role":32,"phone":60,"phoneExt":18,"email":61},"CC Foo","85222554389","ccfoo@hku.hk",{"type":63,"investigatorFullName":18,"investigatorTitle":18,"investigatorAffiliation":18,"oldNameTitle":18,"oldOrganization":18},"SPONSOR",[65],{"name":66,"class":67},"Health and Medical Research Fund","OTHER_GOV","100530020","implementation-and-evaluation-of-a-fear-of-cancer-recurrence-screening-referral-and-management-program-100530020",false,"NCT06181344","Implementation and Evaluation of a Fear of Cancer Recurrence Screening, Referral and Management Program","Implementation and Evaluation of a Fear of Cancer Recurrence Screening, Referral and Management Program for Chinese Cancer Survivors: a Stepped Wedge and Cluster Randomized Trial","Inclusion Criteria:\n\n* All patients diagnosed with non-metastatic breast, gynecological, or colorectal cancer, and who have completed primary and adjuvant treatment within the past two years will be eligible for the proposed screening program.\n\nExclusion Criteria:\n\n* All cancer patients beyond two years post-treatment; and diagnosed with metastatic cancer or non-breast, non-gynecological, and non-colorectal cancer.","ALL","18 Years",{"count":78,"type":79},1980,"ESTIMATED","INTERVENTIONAL",[82],"NA","The purpose of this study is to evaluate the process and outcomes of an implementation program designed to implement fear of cancer screening, referral and management into routine cancer care clinics, using a stepped-wedge cluster randomized controlled trial.",[85,86],"Fear of Cancer Recurrence","Cancer",[88,89],"implementation study","Screening and referral program","2025-01-09",{"date":92,"type":93},"2025-01-13","ACTUAL",{"date":95,"type":93},"2024-07-26",{"date":97,"type":79},"2026-08-31",{"name":5,"class":6},2]